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Alpha7 Nicotinic Acetylcholine Receptor Is a Target in Pharmacology and Toxicology

Alpha7 nicotinic acetylcholine receptor (α7 nAChR) is an important part of the cholinergic nerve system in the brain. Moreover, it is associated with a cholinergic anti-inflammatory pathway in the termination of the parasympathetic nervous system. Antagonists of α7 nAChR are a wide group represented...

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Autor principal: Pohanka, Miroslav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3292018/
https://www.ncbi.nlm.nih.gov/pubmed/22408449
http://dx.doi.org/10.3390/ijms13022219
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author Pohanka, Miroslav
author_facet Pohanka, Miroslav
author_sort Pohanka, Miroslav
collection PubMed
description Alpha7 nicotinic acetylcholine receptor (α7 nAChR) is an important part of the cholinergic nerve system in the brain. Moreover, it is associated with a cholinergic anti-inflammatory pathway in the termination of the parasympathetic nervous system. Antagonists of α7 nAChR are a wide group represented by conotoxin and bungarotoxin. Even Alzheimer’s disease drug memantine acting as an antagonist in its side pathway belongs in this group. Agonists of α7 nAChR are suitable for treatment of multiple cognitive dysfunctions such as Alzheimer’s disease or schizophrenia. Inflammation or even sepsis can be ameliorated by the agonistic acting compounds. Preparations RG3487, SEN34625/WYE-103914, SEN12333, ABT-107, Clozapine, GTS-21, CNI-1493, and AR-R17779 are representative examples of the novel compounds with affinity toward the α7 nAChR. Pharmacological, toxicological, and medicinal significance of α7 nAChR are discussed throughout this paper.
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spelling pubmed-32920182012-03-09 Alpha7 Nicotinic Acetylcholine Receptor Is a Target in Pharmacology and Toxicology Pohanka, Miroslav Int J Mol Sci Review Alpha7 nicotinic acetylcholine receptor (α7 nAChR) is an important part of the cholinergic nerve system in the brain. Moreover, it is associated with a cholinergic anti-inflammatory pathway in the termination of the parasympathetic nervous system. Antagonists of α7 nAChR are a wide group represented by conotoxin and bungarotoxin. Even Alzheimer’s disease drug memantine acting as an antagonist in its side pathway belongs in this group. Agonists of α7 nAChR are suitable for treatment of multiple cognitive dysfunctions such as Alzheimer’s disease or schizophrenia. Inflammation or even sepsis can be ameliorated by the agonistic acting compounds. Preparations RG3487, SEN34625/WYE-103914, SEN12333, ABT-107, Clozapine, GTS-21, CNI-1493, and AR-R17779 are representative examples of the novel compounds with affinity toward the α7 nAChR. Pharmacological, toxicological, and medicinal significance of α7 nAChR are discussed throughout this paper. Molecular Diversity Preservation International (MDPI) 2012-02-17 /pmc/articles/PMC3292018/ /pubmed/22408449 http://dx.doi.org/10.3390/ijms13022219 Text en © 2012 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0 This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Pohanka, Miroslav
Alpha7 Nicotinic Acetylcholine Receptor Is a Target in Pharmacology and Toxicology
title Alpha7 Nicotinic Acetylcholine Receptor Is a Target in Pharmacology and Toxicology
title_full Alpha7 Nicotinic Acetylcholine Receptor Is a Target in Pharmacology and Toxicology
title_fullStr Alpha7 Nicotinic Acetylcholine Receptor Is a Target in Pharmacology and Toxicology
title_full_unstemmed Alpha7 Nicotinic Acetylcholine Receptor Is a Target in Pharmacology and Toxicology
title_short Alpha7 Nicotinic Acetylcholine Receptor Is a Target in Pharmacology and Toxicology
title_sort alpha7 nicotinic acetylcholine receptor is a target in pharmacology and toxicology
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3292018/
https://www.ncbi.nlm.nih.gov/pubmed/22408449
http://dx.doi.org/10.3390/ijms13022219
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